JPH0461035B2 - - Google Patents
Info
- Publication number
- JPH0461035B2 JPH0461035B2 JP57111689A JP11168982A JPH0461035B2 JP H0461035 B2 JPH0461035 B2 JP H0461035B2 JP 57111689 A JP57111689 A JP 57111689A JP 11168982 A JP11168982 A JP 11168982A JP H0461035 B2 JPH0461035 B2 JP H0461035B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- hydrogen atom
- atom
- liquid crystal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004973 liquid crystal related substance Substances 0.000 claims description 58
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 39
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 21
- 125000003545 alkoxy group Chemical group 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 125000003277 amino group Chemical group 0.000 claims description 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 239000000975 dye Substances 0.000 description 67
- 238000010521 absorption reaction Methods 0.000 description 10
- 239000000758 substrate Substances 0.000 description 9
- -1 propylcyclohexyl group Chemical group 0.000 description 8
- 238000000862 absorption spectrum Methods 0.000 description 7
- 125000004663 dialkyl amino group Chemical group 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 5
- 239000004988 Nematic liquid crystal Substances 0.000 description 4
- 238000002835 absorbance Methods 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000013543 active substance Substances 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- DTGKSKDOIYIVQL-NQMVMOMDSA-N (+)-Borneol Natural products C1C[C@]2(C)[C@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-NQMVMOMDSA-N 0.000 description 1
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
- 125000001331 3-methylbutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])O* 0.000 description 1
- 125000005917 3-methylpentyl group Chemical group 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- NEHNMFOYXAPHSD-UHFFFAOYSA-N beta-citronellal Natural products O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000003098 cholesteric effect Effects 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000004915 dibutylamino group Chemical group C(CCC)N(CCCC)* 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
Landscapes
- Liquid Crystal (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11168982A JPS594674A (ja) | 1982-06-30 | 1982-06-30 | ゲスト―ホスト型液晶組成物 |
| US06/509,051 US4588517A (en) | 1982-06-30 | 1983-06-29 | Liquid crystal composition |
| EP83106353A EP0098522B1 (en) | 1982-06-30 | 1983-06-29 | Liquid crystal composition |
| DE8383106353T DE3380031D1 (en) | 1982-06-30 | 1983-06-29 | Liquid crystal composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11168982A JPS594674A (ja) | 1982-06-30 | 1982-06-30 | ゲスト―ホスト型液晶組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS594674A JPS594674A (ja) | 1984-01-11 |
| JPH0461035B2 true JPH0461035B2 (pt) | 1992-09-29 |
Family
ID=14567672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11168982A Granted JPS594674A (ja) | 1982-06-30 | 1982-06-30 | ゲスト―ホスト型液晶組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS594674A (pt) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103336325A (zh) * | 2012-02-28 | 2013-10-02 | 住友化学株式会社 | 偏光膜、圆偏振板及它们的制造方法 |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0635552B2 (ja) * | 1985-06-11 | 1994-05-11 | 三井東圧化学株式会社 | 二色性ジスアゾ色素 |
| JPH0653854B2 (ja) * | 1985-05-31 | 1994-07-20 | 三井東圧化学株式会社 | 液晶表示用ポリアゾ系二色性色素 |
| JPH0662868B2 (ja) * | 1985-01-30 | 1994-08-17 | 三井東圧化学株式会社 | 液晶表示用二色性トリスアゾ色素 |
| JP2579796B2 (ja) * | 1988-03-12 | 1997-02-12 | ダイソー株式会社 | チオインジコ誘導体 |
| JPH086047B2 (ja) * | 1994-03-07 | 1996-01-24 | 三井東圧化学株式会社 | 液晶表示用二色性トリスアゾ色素 |
| US5805528A (en) * | 1996-03-05 | 1998-09-08 | Furuno Electric Co., Ltd. | Underwater detection system |
| JP5203030B2 (ja) * | 2008-04-25 | 2013-06-05 | 京セラドキュメントソリューションズ株式会社 | 電子写真感光体 |
| TWI561588B (en) * | 2011-10-22 | 2016-12-11 | Archroma Ip Gmbh | Trisazo acid dyes |
| JP2019214691A (ja) * | 2018-06-14 | 2019-12-19 | 山本化成株式会社 | 二色性化合物、液晶組成物および液晶素子 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5738857A (en) * | 1980-06-30 | 1982-03-03 | Gen Electric | Trisazo dye for liquid crystal composition |
| JPS57212283A (en) * | 1981-06-13 | 1982-12-27 | Bayer Ag | Azo dye-free liquid crystal substance |
-
1982
- 1982-06-30 JP JP11168982A patent/JPS594674A/ja active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5738857A (en) * | 1980-06-30 | 1982-03-03 | Gen Electric | Trisazo dye for liquid crystal composition |
| JPS57212283A (en) * | 1981-06-13 | 1982-12-27 | Bayer Ag | Azo dye-free liquid crystal substance |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103336325A (zh) * | 2012-02-28 | 2013-10-02 | 住友化学株式会社 | 偏光膜、圆偏振板及它们的制造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS594674A (ja) | 1984-01-11 |
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